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NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease

Nucleotide binding oligomerization domain 2 (NOD2) is an intracellular sensor for small peptides derived from the bacterial cell wall component, peptidoglycan. Recent studies have uncovered unexpected functions of NOD2 in innate immune responses such as induction of type I IFN and facilitation of au...

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Detalles Bibliográficos
Autores principales: Strober, Warren, Watanabe, Tomohiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3773501/
https://www.ncbi.nlm.nih.gov/pubmed/21750585
http://dx.doi.org/10.1038/mi.2011.29
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author Strober, Warren
Watanabe, Tomohiro
author_facet Strober, Warren
Watanabe, Tomohiro
author_sort Strober, Warren
collection PubMed
description Nucleotide binding oligomerization domain 2 (NOD2) is an intracellular sensor for small peptides derived from the bacterial cell wall component, peptidoglycan. Recent studies have uncovered unexpected functions of NOD2 in innate immune responses such as induction of type I IFN and facilitation of autophagy; moreover, they have disclosed extensive cross-talk between NOD2 and Toll-like receptors which plays an indispensable role both in host defense against microbial infection and in the development of autoimmunity. Of particular interest, polymorphisms of CARD15 encoding NOD2 are associated with Crohn's disease and other autoimmune states such as graft versus host disease. In this review, we summarize recent findings regarding normal functions of NOD2 and discuss the mechanisms by which NOD2 polymorphisms associated with Crohn's disease lead to intestinal inflammation.
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spelling pubmed-37735012013-09-15 NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease Strober, Warren Watanabe, Tomohiro Mucosal Immunol Article Nucleotide binding oligomerization domain 2 (NOD2) is an intracellular sensor for small peptides derived from the bacterial cell wall component, peptidoglycan. Recent studies have uncovered unexpected functions of NOD2 in innate immune responses such as induction of type I IFN and facilitation of autophagy; moreover, they have disclosed extensive cross-talk between NOD2 and Toll-like receptors which plays an indispensable role both in host defense against microbial infection and in the development of autoimmunity. Of particular interest, polymorphisms of CARD15 encoding NOD2 are associated with Crohn's disease and other autoimmune states such as graft versus host disease. In this review, we summarize recent findings regarding normal functions of NOD2 and discuss the mechanisms by which NOD2 polymorphisms associated with Crohn's disease lead to intestinal inflammation. 2011-07-13 2011-09 /pmc/articles/PMC3773501/ /pubmed/21750585 http://dx.doi.org/10.1038/mi.2011.29 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Strober, Warren
Watanabe, Tomohiro
NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease
title NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease
title_full NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease
title_fullStr NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease
title_full_unstemmed NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease
title_short NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease
title_sort nod2, an intracellular innate immune sensor involved in host defense and crohn's disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3773501/
https://www.ncbi.nlm.nih.gov/pubmed/21750585
http://dx.doi.org/10.1038/mi.2011.29
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